KR20060069475A - 세펨 화합물 - Google Patents
세펨 화합물 Download PDFInfo
- Publication number
- KR20060069475A KR20060069475A KR1020067003919A KR20067003919A KR20060069475A KR 20060069475 A KR20060069475 A KR 20060069475A KR 1020067003919 A KR1020067003919 A KR 1020067003919A KR 20067003919 A KR20067003919 A KR 20067003919A KR 20060069475 A KR20060069475 A KR 20060069475A
- Authority
- KR
- South Korea
- Prior art keywords
- amino
- methyl
- tert
- compound
- solution
- Prior art date
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- -1 Cephem compounds Chemical class 0.000 title claims abstract description 272
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 141
- 150000001875 compounds Chemical class 0.000 claims abstract description 119
- 150000003839 salts Chemical class 0.000 claims abstract description 82
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 42
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 30
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 20
- 239000001257 hydrogen Substances 0.000 claims abstract description 20
- 125000006239 protecting group Chemical group 0.000 claims abstract description 14
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 5
- 239000003937 drug carrier Substances 0.000 claims abstract description 3
- 238000004519 manufacturing process Methods 0.000 claims abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 5
- 238000002360 preparation method Methods 0.000 claims description 75
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 63
- 238000006243 chemical reaction Methods 0.000 claims description 59
- 238000000034 method Methods 0.000 claims description 56
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 30
- 125000003118 aryl group Chemical group 0.000 claims description 30
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims description 23
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 22
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 claims description 20
- 125000002252 acyl group Chemical group 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
- 125000003282 alkyl amino group Chemical group 0.000 claims description 10
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 7
- 125000005236 alkanoylamino group Chemical group 0.000 claims description 6
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 6
- 125000004442 acylamino group Chemical group 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- 150000001450 anions Chemical class 0.000 claims description 4
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 4
- 208000035473 Communicable disease Diseases 0.000 claims description 3
- 241001465754 Metazoa Species 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 3
- 239000004599 antimicrobial Substances 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 208000015181 infectious disease Diseases 0.000 claims description 2
- 150000003018 phosphorus compounds Chemical class 0.000 claims 3
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 239000012678 infectious agent Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 223
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 184
- 239000000203 mixture Substances 0.000 description 180
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical class CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 133
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 126
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 102
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 87
- 239000011541 reaction mixture Substances 0.000 description 82
- 239000012267 brine Substances 0.000 description 72
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 72
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 72
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 67
- 239000007787 solid Substances 0.000 description 59
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 57
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 56
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 55
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 53
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 52
- 238000001914 filtration Methods 0.000 description 49
- 239000012043 crude product Substances 0.000 description 48
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 48
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 44
- 239000012044 organic layer Substances 0.000 description 43
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 40
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 36
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 36
- 239000002244 precipitate Substances 0.000 description 36
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 35
- 239000012141 concentrate Substances 0.000 description 34
- 235000008504 concentrate Nutrition 0.000 description 34
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 34
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 32
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 31
- 239000002904 solvent Substances 0.000 description 31
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 28
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 28
- 239000000706 filtrate Substances 0.000 description 28
- 230000002829 reductive effect Effects 0.000 description 28
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 28
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 27
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 26
- 239000003921 oil Substances 0.000 description 26
- 235000019198 oils Nutrition 0.000 description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 25
- 239000011734 sodium Substances 0.000 description 25
- 235000015165 citric acid Nutrition 0.000 description 24
- 239000000741 silica gel Substances 0.000 description 24
- 229910002027 silica gel Inorganic materials 0.000 description 24
- 238000004440 column chromatography Methods 0.000 description 23
- 238000002953 preparative HPLC Methods 0.000 description 23
- 239000002253 acid Substances 0.000 description 22
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 21
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 20
- 235000017557 sodium bicarbonate Nutrition 0.000 description 20
- 239000000725 suspension Substances 0.000 description 20
- 229920006395 saturated elastomer Polymers 0.000 description 18
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 18
- 239000000047 product Substances 0.000 description 17
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 16
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 15
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 15
- UYCAUPASBSROMS-AWQJXPNKSA-M sodium;2,2,2-trifluoroacetate Chemical compound [Na+].[O-][13C](=O)[13C](F)(F)F UYCAUPASBSROMS-AWQJXPNKSA-M 0.000 description 15
- JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 0.000 description 15
- 239000003054 catalyst Substances 0.000 description 13
- LWFWUJCJKPUZLV-UHFFFAOYSA-N n-trimethylsilylacetamide Chemical compound CC(=O)N[Si](C)(C)C LWFWUJCJKPUZLV-UHFFFAOYSA-N 0.000 description 13
- 229910052763 palladium Inorganic materials 0.000 description 13
- 238000010992 reflux Methods 0.000 description 13
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 12
- 238000003756 stirring Methods 0.000 description 12
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 12
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 11
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 11
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 11
- 238000000746 purification Methods 0.000 description 11
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 9
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 8
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 8
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 8
- 239000012298 atmosphere Substances 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 239000003610 charcoal Substances 0.000 description 8
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 8
- 125000001841 imino group Chemical group [H]N=* 0.000 description 8
- 239000010410 layer Substances 0.000 description 8
- 238000006722 reduction reaction Methods 0.000 description 8
- 235000011054 acetic acid Nutrition 0.000 description 7
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 238000010792 warming Methods 0.000 description 7
- CIMLJTZGZLWBJY-UHFFFAOYSA-N 2-methylpyrazole-3,4-diamine;sulfuric acid Chemical compound OS(O)(=O)=O.CN1N=CC(N)=C1N CIMLJTZGZLWBJY-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 0 CC1C*(C)CCC1 Chemical compound CC1C*(C)CCC1 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 230000007062 hydrolysis Effects 0.000 description 6
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- 150000007529 inorganic bases Chemical class 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 239000012046 mixed solvent Substances 0.000 description 6
- JQUGGROFFNEWEN-UHFFFAOYSA-N phenyl n-[1-methyl-5-(tritylamino)pyrazol-4-yl]carbamate Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)NC=1N(C)N=CC=1NC(=O)OC1=CC=CC=C1 JQUGGROFFNEWEN-UHFFFAOYSA-N 0.000 description 6
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 5
- 230000002411 adverse Effects 0.000 description 5
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- WDCDAAMJNUHOIY-UHFFFAOYSA-N ethyl acetate;2-propan-2-yloxypropane Chemical compound CCOC(C)=O.CC(C)OC(C)C WDCDAAMJNUHOIY-UHFFFAOYSA-N 0.000 description 5
- 150000007530 organic bases Chemical class 0.000 description 5
- 229910052697 platinum Inorganic materials 0.000 description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- KNORWRWRHNHJAV-UHFFFAOYSA-N tert-butyl n-[2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethylamino]ethyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCNCCNC(=O)OC(C)(C)C KNORWRWRHNHJAV-UHFFFAOYSA-N 0.000 description 5
- GOQZIPJCBUYLIR-UHFFFAOYSA-N tert-butyl n-[n-[(2-methylpropan-2-yl)oxycarbonyl]-n'-(trifluoromethylsulfonyl)carbamimidoyl]carbamate Chemical compound CC(C)(C)OC(=O)NC(=NS(=O)(=O)C(F)(F)F)NC(=O)OC(C)(C)C GOQZIPJCBUYLIR-UHFFFAOYSA-N 0.000 description 5
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 5
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 5
- MASDFXZJIDNRTR-UHFFFAOYSA-N 1,3-bis(trimethylsilyl)urea Chemical compound C[Si](C)(C)NC(=O)N[Si](C)(C)C MASDFXZJIDNRTR-UHFFFAOYSA-N 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 239000002841 Lewis acid Substances 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N Valeric acid Natural products CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 4
- 125000004423 acyloxy group Chemical group 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 150000007517 lewis acids Chemical class 0.000 description 4
- 244000000010 microbial pathogen Species 0.000 description 4
- 150000007522 mineralic acids Chemical class 0.000 description 4
- 235000019260 propionic acid Nutrition 0.000 description 4
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 4
- 239000006104 solid solution Substances 0.000 description 4
- AOCSUUGBCMTKJH-UHFFFAOYSA-N tert-butyl n-(2-aminoethyl)carbamate Chemical compound CC(C)(C)OC(=O)NCCN AOCSUUGBCMTKJH-UHFFFAOYSA-N 0.000 description 4
- GJDVUJONFOURFS-JTQLQIEISA-N tert-butyl n-[(5s)-5-amino-6-[(5-amino-1-methylpyrazol-4-yl)amino]-6-oxohexyl]carbamate Chemical compound CN1N=CC(NC(=O)[C@@H](N)CCCCNC(=O)OC(C)(C)C)=C1N GJDVUJONFOURFS-JTQLQIEISA-N 0.000 description 4
- QYVFEFFJTQKDTK-UHFFFAOYSA-N tert-butyl n-[2-amino-3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]carbamate Chemical compound CC(C)(C)OC(=O)NCC(N)CNC(=O)OC(C)(C)C QYVFEFFJTQKDTK-UHFFFAOYSA-N 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 125000006624 (C1-C6) alkoxycarbonylamino group Chemical group 0.000 description 3
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 3
- BCEYYHSFRGXEHZ-UHFFFAOYSA-N 1,3-bis[(2-methylpropan-2-yl)oxycarbonylamino]propan-2-yl methanesulfonate Chemical compound CC(C)(C)OC(=O)NCC(OS(C)(=O)=O)CNC(=O)OC(C)(C)C BCEYYHSFRGXEHZ-UHFFFAOYSA-N 0.000 description 3
- YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-UHFFFAOYSA-N 0.000 description 3
- GUPBEFNIQBAMBP-UHFFFAOYSA-N 2-methyl-3-n-tritylpyrazole-3,4-diamine Chemical compound CN1N=CC(N)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 GUPBEFNIQBAMBP-UHFFFAOYSA-N 0.000 description 3
- JESRNIJXVIFVOV-UHFFFAOYSA-N 2-methylpyrazol-3-amine Chemical compound CN1N=CC=C1N JESRNIJXVIFVOV-UHFFFAOYSA-N 0.000 description 3
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical class CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 3
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 3
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
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- VTIZPJJBPVMLRT-UHFFFAOYSA-N heptane;2-propan-2-yloxypropane Chemical compound CCCCCCC.CC(C)OC(C)C VTIZPJJBPVMLRT-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 229910003480 inorganic solid Inorganic materials 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000005929 isobutyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])OC(*)=O 0.000 description 1
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 235000015122 lemonade Nutrition 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005905 mesyloxy group Chemical class 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- DFCDLLNULGMFAS-UHFFFAOYSA-N n'-tritylethane-1,2-diamine Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(NCCN)C1=CC=CC=C1 DFCDLLNULGMFAS-UHFFFAOYSA-N 0.000 description 1
- UHAAFJWANJYDIS-UHFFFAOYSA-N n,n'-diethylmethanediimine Chemical compound CCN=C=NCC UHAAFJWANJYDIS-UHFFFAOYSA-N 0.000 description 1
- VMESOKCXSYNAKD-UHFFFAOYSA-N n,n-dimethylhydroxylamine Chemical compound CN(C)O VMESOKCXSYNAKD-UHFFFAOYSA-N 0.000 description 1
- JVHPKYBRJQNPAT-UHFFFAOYSA-N n-cyclohexyl-2,2-diphenylethenimine Chemical compound C1CCCCC1N=C=C(C=1C=CC=CC=1)C1=CC=CC=C1 JVHPKYBRJQNPAT-UHFFFAOYSA-N 0.000 description 1
- 125000001038 naphthoyl group Chemical group C1(=CC=CC2=CC=CC=C12)C(=O)* 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- 229910003445 palladium oxide Inorganic materials 0.000 description 1
- JQPTYAILLJKUCY-UHFFFAOYSA-N palladium(ii) oxide Chemical compound [O-2].[Pd+2] JQPTYAILLJKUCY-UHFFFAOYSA-N 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- MYDQAEQZZKVJSL-UHFFFAOYSA-N pentyl carbamate Chemical compound CCCCCOC(N)=O MYDQAEQZZKVJSL-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000001148 pentyloxycarbonyl group Chemical group 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- AHWALFGBDFAJAI-UHFFFAOYSA-N phenyl carbonochloridate Chemical compound ClC(=O)OC1=CC=CC=C1 AHWALFGBDFAJAI-UHFFFAOYSA-N 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- FYRHIOVKTDQVFC-UHFFFAOYSA-M potassium phthalimide Chemical compound [K+].C1=CC=C2C(=O)[N-]C(=O)C2=C1 FYRHIOVKTDQVFC-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 229940116357 potassium thiocyanate Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- IVRIRQXJSNCSPQ-UHFFFAOYSA-N propan-2-yl carbonochloridate Chemical compound CC(C)OC(Cl)=O IVRIRQXJSNCSPQ-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000006633 tert-butoxycarbonylamino group Chemical group 0.000 description 1
- NMPXNRGQIFCZOQ-ZDUSSCGKSA-N tert-butyl n-[(2s)-1-[(5-amino-1-methylpyrazol-4-yl)amino]-6-[(2-methylpropan-2-yl)oxycarbonylamino]-1-oxohexan-2-yl]carbamate Chemical compound CN1N=CC(NC(=O)[C@H](CCCCNC(=O)OC(C)(C)C)NC(=O)OC(C)(C)C)=C1N NMPXNRGQIFCZOQ-ZDUSSCGKSA-N 0.000 description 1
- ZPNGEQYJYGOBGB-LJAQVGFWSA-N tert-butyl n-[(2s)-4-[(2-methylpropan-2-yl)oxycarbonylamino]-1-[[1-methyl-5-(tritylamino)pyrazol-4-yl]amino]-1-oxobutan-2-yl]carbamate Chemical compound CN1N=CC(NC(=O)[C@H](CCNC(=O)OC(C)(C)C)NC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 ZPNGEQYJYGOBGB-LJAQVGFWSA-N 0.000 description 1
- ZTHSFXGTMVXABM-HKBQPEDESA-N tert-butyl n-[(2s)-6-[(2-methylpropan-2-yl)oxycarbonylamino]-1-[[1-methyl-5-(tritylamino)pyrazol-4-yl]amino]-1-oxohexan-2-yl]carbamate Chemical compound CN1N=CC(NC(=O)[C@H](CCCCNC(=O)OC(C)(C)C)NC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 ZTHSFXGTMVXABM-HKBQPEDESA-N 0.000 description 1
- AKZKZLGOIWNLEM-NDEPHWFRSA-N tert-butyl n-[(3s)-3-hydroxy-4-[[1-(2-hydroxyethyl)-5-(tritylamino)pyrazol-4-yl]amino]-4-oxobutyl]carbamate Chemical compound C1=NN(CCO)C(NC(C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1NC(=O)[C@@H](O)CCNC(=O)OC(C)(C)C AKZKZLGOIWNLEM-NDEPHWFRSA-N 0.000 description 1
- SCLDCYMJRSCIIC-MHZLTWQESA-N tert-butyl n-[(3s)-3-hydroxy-4-[[1-methyl-5-(tritylamino)pyrazol-4-yl]amino]-4-oxobutyl]carbamate Chemical compound CN1N=CC(NC(=O)[C@@H](O)CCNC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 SCLDCYMJRSCIIC-MHZLTWQESA-N 0.000 description 1
- CTSCZFSUTLRAAQ-XIFFEERXSA-N tert-butyl n-[(4s)-4-[bis[(2-methylpropan-2-yl)oxycarbonylamino]methylideneamino]-5-[[1-methyl-5-(tritylamino)pyrazol-4-yl]amino]-5-oxopentyl]carbamate Chemical compound CN1N=CC(NC(=O)[C@H](CCCNC(=O)OC(C)(C)C)NC(NC(=O)OC(C)(C)C)=NC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CTSCZFSUTLRAAQ-XIFFEERXSA-N 0.000 description 1
- WZZWFACKEDQAHX-MHZLTWQESA-N tert-butyl n-[(4s)-4-amino-5-[[1-methyl-5-(tritylamino)pyrazol-4-yl]amino]-5-oxopentyl]carbamate Chemical compound CN1N=CC(NC(=O)[C@@H](N)CCCNC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 WZZWFACKEDQAHX-MHZLTWQESA-N 0.000 description 1
- KWKNLHZCQPECRK-UMSFTDKQSA-N tert-butyl n-[(5s)-5-[bis[(2-methylpropan-2-yl)oxycarbonylamino]methylideneamino]-6-[[1-methyl-5-(tritylamino)pyrazol-4-yl]amino]-6-oxohexyl]carbamate Chemical compound CN1N=CC(NC(=O)[C@H](CCCCNC(=O)OC(C)(C)C)NC(NC(=O)OC(C)(C)C)=NC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 KWKNLHZCQPECRK-UMSFTDKQSA-N 0.000 description 1
- LAPIGCNZTNCSIB-LKUDQCMESA-N tert-butyl n-[(e)-4-cyano-3-[[1-methyl-5-(tritylamino)pyrazol-4-yl]carbamoyl]but-3-enyl]carbamate Chemical compound CN1N=CC(NC(=O)C(\CCNC(=O)OC(C)(C)C)=C\C#N)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 LAPIGCNZTNCSIB-LKUDQCMESA-N 0.000 description 1
- CLPRXUCBOBBWTE-UHFFFAOYSA-N tert-butyl n-[2-(1,3-dioxoisoindol-2-yl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]carbamate Chemical compound C1=CC=C2C(=O)N(C(CNC(=O)OC(C)(C)C)CNC(=O)OC(C)(C)C)C(=O)C2=C1 CLPRXUCBOBBWTE-UHFFFAOYSA-N 0.000 description 1
- STBFLSBYUBVMET-UHFFFAOYSA-N tert-butyl n-[2-[2-(tritylamino)ethylamino]ethyl]carbamate Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(NCCNCCNC(=O)OC(C)(C)C)C1=CC=CC=C1 STBFLSBYUBVMET-UHFFFAOYSA-N 0.000 description 1
- NMVGNDUTKSVHOB-UHFFFAOYSA-N tert-butyl n-[2-[3-(tritylamino)propylamino]ethyl]carbamate Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(NCCCNCCNC(=O)OC(C)(C)C)C1=CC=CC=C1 NMVGNDUTKSVHOB-UHFFFAOYSA-N 0.000 description 1
- WXSYWZSVICRHCP-UHFFFAOYSA-N tert-butyl n-[2-[[1-(2-hydroxyethyl)-5-(tritylamino)pyrazol-4-yl]carbamoylamino]-3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]carbamate Chemical compound C1=NN(CCO)C(NC(C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1NC(=O)NC(CNC(=O)OC(C)(C)C)CNC(=O)OC(C)(C)C WXSYWZSVICRHCP-UHFFFAOYSA-N 0.000 description 1
- VUOFFUJGRSHEHS-UHFFFAOYSA-N tert-butyl n-[2-[[1-methyl-5-(tritylamino)pyrazol-4-yl]carbamoyl-[2-(tritylamino)ethyl]amino]ethyl]carbamate Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)NC=1N(C)N=CC=1NC(=O)N(CCNC(=O)OC(C)(C)C)CCNC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 VUOFFUJGRSHEHS-UHFFFAOYSA-N 0.000 description 1
- HCSFVIXXFWFMRY-UHFFFAOYSA-N tert-butyl n-[2-[[1-methyl-5-(tritylamino)pyrazol-4-yl]carbamoyl-[3-(tritylamino)propyl]amino]ethyl]carbamate Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)NC=1N(C)N=CC=1NC(=O)N(CCNC(=O)OC(C)(C)C)CCCNC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 HCSFVIXXFWFMRY-UHFFFAOYSA-N 0.000 description 1
- CXYHBACXYGGHPI-UHFFFAOYSA-N tert-butyl n-[2-[[2-amino-3-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethylamino]-3-oxopropanoyl]amino]ethyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCNC(=O)C(N)C(=O)NCCNC(=O)OC(C)(C)C CXYHBACXYGGHPI-UHFFFAOYSA-N 0.000 description 1
- DJPSHOUXODCGGX-UHFFFAOYSA-N tert-butyl n-[2-[[3-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethylamino]-2-[[1-methyl-5-(tritylamino)pyrazol-4-yl]carbamoylamino]-3-oxopropanoyl]amino]ethyl]carbamate Chemical compound CN1N=CC(NC(=O)NC(C(=O)NCCNC(=O)OC(C)(C)C)C(=O)NCCNC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 DJPSHOUXODCGGX-UHFFFAOYSA-N 0.000 description 1
- RUZXBPVPRGXEAI-UHFFFAOYSA-N tert-butyl n-[3-[(2-methylpropan-2-yl)oxycarbonylamino]-2-[1-methyl-5-(tritylamino)pyrazol-4-yl]propyl]carbamate Chemical compound CN1N=CC(C(CNC(=O)OC(C)(C)C)CNC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 RUZXBPVPRGXEAI-UHFFFAOYSA-N 0.000 description 1
- WOSZSCSQONLHGQ-UHFFFAOYSA-N tert-butyl n-[3-[(2-methylpropan-2-yl)oxycarbonylamino]-2-[[3-[[1-methyl-5-(tritylamino)pyrazol-4-yl]amino]-3-oxopropanoyl]amino]propyl]carbamate Chemical compound CN1N=CC(NC(=O)CC(=O)NC(CNC(=O)OC(C)(C)C)CNC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 WOSZSCSQONLHGQ-UHFFFAOYSA-N 0.000 description 1
- YQMXYCMKAWSWQB-UHFFFAOYSA-N tert-butyl n-[3-[(2-methylpropan-2-yl)oxycarbonylamino]-2-oxopropyl]carbamate Chemical compound CC(C)(C)OC(=O)NCC(=O)CNC(=O)OC(C)(C)C YQMXYCMKAWSWQB-UHFFFAOYSA-N 0.000 description 1
- UYGMYVPMLFZWTH-XIFFEERXSA-N tert-butyl n-[3-[[(2s)-6-[(2-methylpropan-2-yl)oxycarbonylamino]-1-[[1-methyl-5-(tritylamino)pyrazol-4-yl]amino]-1-oxohexan-2-yl]amino]-3-oxopropyl]carbamate Chemical compound CN1N=CC(NC(=O)[C@H](CCCCNC(=O)OC(C)(C)C)NC(=O)CCNC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 UYGMYVPMLFZWTH-XIFFEERXSA-N 0.000 description 1
- XAMNUJSMTRRXSD-UHFFFAOYSA-N tert-butyl n-[5-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[[1-methyl-5-(tritylamino)pyrazol-4-yl]carbamoyl]pentyl]carbamate Chemical compound CN1N=CC(NC(=O)C(CCNC(=O)OC(C)(C)C)CCNC(=O)OC(C)(C)C)=C1NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 XAMNUJSMTRRXSD-UHFFFAOYSA-N 0.000 description 1
- VXMZANCVXCVRBJ-UHFFFAOYSA-N tert-butyl n-[n-[(5-amino-1-methylpyrazol-4-yl)methyl]-n'-[(2-methylpropan-2-yl)oxycarbonyl]-n-[2-(tritylamino)ethyl]carbamimidoyl]carbamate Chemical compound CN1N=CC(CN(CCNC(C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)C(NC(=O)OC(C)(C)C)=NC(=O)OC(C)(C)C)=C1N VXMZANCVXCVRBJ-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000001974 tryptic soy broth Substances 0.000 description 1
- 108010050327 trypticase-soy broth Proteins 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/14—Compounds having a nitrogen atom directly attached in position 7
- C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
- C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
- C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
- A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
- A61K31/546—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine containing further heterocyclic rings, e.g. cephalothin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2003905084 | 2003-09-18 | ||
| AU2003905084A AU2003905084A0 (en) | 2003-09-18 | Cephem Compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20060069475A true KR20060069475A (ko) | 2006-06-21 |
Family
ID=34318291
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020067003919A KR20060069475A (ko) | 2003-09-18 | 2004-09-17 | 세펨 화합물 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7192943B2 (de) |
| EP (1) | EP1663245B1 (de) |
| JP (1) | JP4643577B2 (de) |
| KR (1) | KR20060069475A (de) |
| CN (1) | CN1852715A (de) |
| AR (1) | AR045768A1 (de) |
| AT (1) | ATE463248T1 (de) |
| CA (1) | CA2536636A1 (de) |
| DE (1) | DE602004026451D1 (de) |
| ES (1) | ES2340928T3 (de) |
| MX (1) | MXPA06003068A (de) |
| TW (1) | TW200524943A (de) |
| WO (1) | WO2005027909A1 (de) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20030090794A (ko) * | 2001-05-01 | 2003-11-28 | 후지사와 야꾸힝 고교 가부시키가이샤 | 세펨 화합물 |
| DK1556389T6 (da) * | 2002-10-30 | 2015-05-11 | Astellas Pharma Inc | Cephemforbindelser |
| AU2003902380A0 (en) * | 2003-05-16 | 2003-06-05 | Fujisawa Pharmaceutical Co., Ltd. | Cephem compounds |
| EP1994035A1 (de) * | 2006-03-16 | 2008-11-26 | Astellas Pharma Inc. | Cephemverbindungen und ihre verwendung als antimikrobiotika |
| US7956185B2 (en) * | 2006-05-26 | 2011-06-07 | Abbott Laboratories | Cyclobut-3-ene-1,2,-dione inhibitors of polo-like kinases |
| EA028342B1 (ru) | 2011-09-09 | 2017-11-30 | Мерк Шарп И Доум Корп. | Способы лечения пневмонии |
| US8809314B1 (en) | 2012-09-07 | 2014-08-19 | Cubist Pharmacueticals, Inc. | Cephalosporin compound |
| US8476425B1 (en) | 2012-09-27 | 2013-07-02 | Cubist Pharmaceuticals, Inc. | Tazobactam arginine compositions |
| WO2014152763A1 (en) | 2013-03-14 | 2014-09-25 | Cubist Pharmaceuticals, Inc. | Cephalosporin compositions and methods of manufacture |
| US20140274996A1 (en) | 2013-03-15 | 2014-09-18 | Cubist Pharmaceuticals, Inc. | Tazobactam and ceftolozane antibiotic compositions |
| US20140274994A1 (en) | 2013-03-15 | 2014-09-18 | Cubist Pharmaceuticals, Inc. | Stabilizing ceftolozane |
| US9872906B2 (en) | 2013-03-15 | 2018-01-23 | Merck Sharp & Dohme Corp. | Ceftolozane antibiotic compositions |
| EP3043797B1 (de) | 2013-09-09 | 2020-04-08 | Merck Sharp & Dohme Corp. | Behandlung von infektionen mit ceftolozan/tazobactam bei personen mit beeinträchtigter nierenfunktion |
| US20150094293A1 (en) | 2013-09-27 | 2015-04-02 | Calixa Therapeutics, Inc. | Solid forms of ceftolozane |
| WO2015196077A1 (en) * | 2014-06-20 | 2015-12-23 | Merck Sharp & Dohme Corp. | Reactions of thiadiazolyl-oximinoacetic acid derivative compounds |
| CN110204558B (zh) | 2014-08-15 | 2022-05-06 | 默沙东公司 | 头孢菌素化合物的合成 |
| WO2016025813A1 (en) | 2014-08-15 | 2016-02-18 | Merck Sharp & Dohme Corp. | Intermediates in the synthesis of cephalosporin compounds |
| WO2016028670A1 (en) | 2014-08-18 | 2016-02-25 | Merck Sharp & Dohme Corp. | Salt forms of ceftolozane |
| US10059680B2 (en) | 2014-12-18 | 2018-08-28 | Merck Sharp & Dohme Corp. | Thiadiazolyl-oximinoacetic acid derivative compounds |
| WO2016095860A1 (en) * | 2014-12-18 | 2016-06-23 | Merck Sharp & Dohme Corp. | Pyrazolyl carboxylic acid and pyrazolyl urea derivative compounds |
| US20160176897A1 (en) | 2014-12-23 | 2016-06-23 | Merck Sharp & Dohme Corp. | 7-aminocephem derivative compounds |
| US10214543B2 (en) | 2014-12-30 | 2019-02-26 | Merck Sharp & Dohme Corp. | Synthesis of cephalosporin compounds |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GR78245B (de) | 1980-09-12 | 1984-09-26 | Ciba Geigy Ag | |
| JPS584789A (ja) * | 1981-04-03 | 1983-01-11 | Fujisawa Pharmaceut Co Ltd | 新規セフエム化合物およびその製造法 |
| DE3279470D1 (en) | 1981-04-03 | 1989-04-06 | Fujisawa Pharmaceutical Co | New cephem compounds, processes for their preparation, pharmaceutical compositions containing them and their starting compounds |
| US5194432A (en) | 1985-11-22 | 1993-03-16 | Fujisawa Pharmaceutical Co., Ltd. | Cephem compounds |
| CA1293719C (en) * | 1986-09-22 | 1991-12-31 | Takao Takaya | Cephem compounds and processes for preparation thereof |
| US5663163A (en) * | 1987-09-07 | 1997-09-02 | Fujisawa Pharmaceutical Co., Ltd. | Cephem compounds and processes for preparation thereof |
| US5210080A (en) * | 1987-09-07 | 1993-05-11 | Fujisawa Pharmaceutical Co., Ltd. | Cephem compounds |
| IE63094B1 (en) * | 1987-09-14 | 1995-03-22 | Fujisawa Pharmaceutical Co | Cephem compound and a process for preparation thereof |
| US5173485A (en) * | 1988-03-09 | 1992-12-22 | Fujisawa Pharmaceutical Company, Ltd. | Cephem compounds |
| GB8805642D0 (en) * | 1988-03-09 | 1988-04-07 | Fujisawa Pharmaceutical Co | New cephem compounds & processes for preparation thereof |
| GB8905301D0 (en) * | 1989-03-08 | 1989-04-19 | Fujisawa Pharmaceutical Co | New cephem compound and a process for preparation thereof |
| US5215982A (en) * | 1989-11-10 | 1993-06-01 | Fujisawa Pharmaceutical Co., Ltd. | Cephem compounds |
| KR910015587A (ko) * | 1990-02-27 | 1991-09-30 | 후지사와 토모키치로 | 세펨 화합물 |
| JPH03255087A (ja) * | 1990-03-05 | 1991-11-13 | Fujisawa Pharmaceut Co Ltd | 新規セフェム化合物およびその塩類 |
| CN1150429A (zh) * | 1994-05-23 | 1997-05-21 | 韩国科学技术研究院 | 头孢菌素化合物及其制备方法 |
| JPH09110877A (ja) | 1995-10-17 | 1997-04-28 | Katayama Seiyakushiyo:Kk | セフェム化合物、その製造法及びそれを含有する抗菌剤 |
| AUPN955596A0 (en) | 1996-04-30 | 1996-05-23 | Fujisawa Pharmaceutical Co., Ltd. | New compound |
| TW526202B (en) * | 1998-11-27 | 2003-04-01 | Shionogi & Amp Co | Broad spectrum cephem having benzo[4,5-b]pyridium methyl group of antibiotic activity |
| KR20030090794A (ko) * | 2001-05-01 | 2003-11-28 | 후지사와 야꾸힝 고교 가부시키가이샤 | 세펨 화합물 |
| DK1556389T6 (da) * | 2002-10-30 | 2015-05-11 | Astellas Pharma Inc | Cephemforbindelser |
| AU2003902380A0 (en) * | 2003-05-16 | 2003-06-05 | Fujisawa Pharmaceutical Co., Ltd. | Cephem compounds |
-
2004
- 2004-09-17 AR ARP040103366A patent/AR045768A1/es unknown
- 2004-09-17 WO PCT/JP2004/014018 patent/WO2005027909A1/en active Application Filing
- 2004-09-17 US US10/942,916 patent/US7192943B2/en not_active Expired - Fee Related
- 2004-09-17 DE DE602004026451T patent/DE602004026451D1/de active Active
- 2004-09-17 EP EP04773402A patent/EP1663245B1/de not_active Not-in-force
- 2004-09-17 CN CNA2004800269008A patent/CN1852715A/zh active Pending
- 2004-09-17 MX MXPA06003068A patent/MXPA06003068A/es not_active Application Discontinuation
- 2004-09-17 CA CA002536636A patent/CA2536636A1/en not_active Abandoned
- 2004-09-17 ES ES04773402T patent/ES2340928T3/es active Active
- 2004-09-17 AT AT04773402T patent/ATE463248T1/de not_active IP Right Cessation
- 2004-09-17 TW TW093128132A patent/TW200524943A/zh unknown
- 2004-09-17 JP JP2006526812A patent/JP4643577B2/ja not_active Expired - Fee Related
- 2004-09-17 KR KR1020067003919A patent/KR20060069475A/ko not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| DE602004026451D1 (de) | 2010-05-20 |
| MXPA06003068A (es) | 2006-08-25 |
| WO2005027909A1 (en) | 2005-03-31 |
| CA2536636A1 (en) | 2005-03-31 |
| TW200524943A (en) | 2005-08-01 |
| JP2007505895A (ja) | 2007-03-15 |
| CN1852715A (zh) | 2006-10-25 |
| US20050096306A1 (en) | 2005-05-05 |
| ES2340928T3 (es) | 2010-06-11 |
| AR045768A1 (es) | 2005-11-09 |
| US7192943B2 (en) | 2007-03-20 |
| EP1663245A1 (de) | 2006-06-07 |
| ATE463248T1 (de) | 2010-04-15 |
| EP1663245B1 (de) | 2010-04-07 |
| JP4643577B2 (ja) | 2011-03-02 |
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| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |